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July 11, 2013 | ISSUE NUMBER 307 VOL 10

Regulatory
Why Patient Adherence is a Policy Issue
Patient non-adherence is costing the US healthcare system nearly $290 billion annually and accounts for approximately 13 percent of the total healthcare expenditures. From a government perspective, the need to rein in healthcare costs, long a political priority for some, is now a fiscal necessity. Joe Ganley outlines some macro trends in public policy that he says will impact adherence significantly ...Read more

Digital Pharma
Is Pinterest the Risk-Free Social Channel for Pharma?
Spoiler Alert: the answer is no, writes Peter Houston. Social media participation is never entirely without risk, but Pinterest presents and intriguing opportunity for Pharma to join the visual web
...Read more

Obamacare
Those Amazing ‘Gold Plated, Cadillac Care’ Drug Programs
Some 20% of Americans enjoy the benefits of a robust, corporate-funded drug benefit plan, but new taxes on so-called ‘Cadillac care’ plans arising from provisions in the Affordable Care Act could take some health insurance beneficiaries – and pharma – by surprise, writes Tom Norton, particularly when coverage decisions, and individual costs, get shifted onto patients
...Read more

Value
For What It’s Worth: Study Probes Evolving Value Schemes
A new study determines that collaboration across three fronts is needed to ensure that value is recognized and adapted over time, taking into account real-world evidence
...Read more

SciVigilance – Pharmacovigilance in a box
Effective safety and risk management is a result of a multi-tiered effort that ensures the safety of a product and mitigates the risks for pharmaceutical companies. While pharmacovigilance depends extensively on human sources for information input and processing of data, the growing volume of data and evolving regulations necessitates robust technology enabled process execution to manage the myriad of risks.Read More

Legal
Lanham Act: Peer Review on Trial
Scientific opinion has special protection under the First Amendment, but does that give pharma a free pass to BYOD – build your own dataset – publish a peer-reviewed article based on the data, and then promote it for competitive advantage? The 2nd US Circuit Court of Appeals weighs in
...Read more

Global
Whatever Happened to Outsourcing in Asia?
Last year, industry research pointed to China and India as the industry's top potential destinations for offshoring over the next five years, which put them ahead of traditional biomanufacturing hubs in the US and Western Europe. A new report, however, suggests that enthusiasm may have diminished
...Read more

//Natale Ricciardi, who retired from Pfizer after 39 years in 2011, joined the board of Dynavax Techonlogies (Berkeley, CA). //Warp Drive Bio (Cambridge, MA) named co-founder Gregory Verdine as CEO, replacing Alexis Brosy, who will become Executive Chairman. The company also hired Dr James Nichols as Chief Operating Officer and added Dr Julian Adams to its Board of Directors. //AMAG Pharmaceuticals (Lexington, MA) appointed Amit Verma as VP,Marketing.//Porgenics Pharmaceuticals (Tarrytown, NY) appointed Hagop Youssoufian as Executive VP, Research & Development.//

July 17–18: CBI’s Orphan Drug Information Summit
Philadelphia, PA.


August 19–21: 7th Annual Forum on Sunshine and Aggregate Spend
Washington DC.


September 18: Life Sciences Financial Transformation Summit
Philadelphia, PA.


 
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